FDA 510(k) Applications Submitted by Christian Muenster

FDA 510(k) Number	Submission Date	Device Name	Applicant
K170171	01/19/2017	IOLMaster 700	Carl Zeiss Meditec AG
K180229	01/26/2018	RESCAN 700, CALLISTO eye	Carl Zeiss Meditec AG
K170638	03/02/2017	Retina Workplace	Carl Zeiss Meditec AG
K170667	03/06/2017	QEVO System with KINEVO 900	Carl Zeiss Meditec AG
K180839	03/30/2018	AT 030	Carl Zeiss Meditec AG
K180858	04/02/2018	CALLISTO eye	Carl Zeiss Meditec AG
K181116	04/27/2018	CONVIVO	Carl Zeiss Meditec AG
K161607	06/10/2016	VISULUX	CARL ZEISS MEDITEC AG
K162568	09/14/2016	INTRABEAM 600	CARL ZEISS MEDITEC AG
K162684	09/26/2016	SL 220	Carl Zeiss Meditec AG
K173771	12/11/2017	IOLMaster 700	Carl Zeiss Meditec AG